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Diallyl disulfide ameliorates isoproterenol induced cardiac hypertrophy activating mitochondrial biogenesis via eNOS-Nrf2-Tfam pathway in rats
Author(s) -
Tarak Nath Khatua,
Amit Kumar Dinda,
Uday Kumar Putcha,
S. Banerjee
Publication year - 2015
Publication title -
biochemistry and biophysics reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.641
H-Index - 23
ISSN - 2405-5808
DOI - 10.1016/j.bbrep.2015.11.008
Subject(s) - tfam , mitochondrial biogenesis , muscle hypertrophy , diallyl disulfide , mitochondrion , medicine , endocrinology , cardioprotection , chemistry , apoptosis , pharmacology , biology , biochemistry , myocardial infarction
The beneficial effect of garlic on cardiovascular disease is well known. However, the use of raw garlic against cardiac hypertrophy is not established. In the present study we explored whether raw garlic and its compound, diallyl disulfide (DADS) could inhibit hypertrophy through H2S and/or mitochondrial biogenesis. Cardiac hypertrophy was induced in rat by giving isoproterenol at the dose of 5 mg/kg/day subcutaneously for 14 days through alzet minipump. Aqueous garlic homogenate, DADS and NaHS (liberate H2S) were fed to third, forth and fifth group of rats for 14 days at a dose of 250 mg/kg/day, 50 mg/kg/day, 14 µM/kg/day respectively. Garlic and DADS reduced cardiac hypertrophy markers and normalized mitochondrial ETC-complex activities, mitochondrial enzyme activites and mitochondrial biogenetic and apoptotic genes expression. Garlic and DADS enhanced eNOS and p-AKT level in rat heart along with increased NRF2 protein level and Tfam gene expression. However, normalization was not observed after administration of NaHS which generates H2S in-vivo. In conclusion, garlic and DADS induces mitochondrial biogenesis and ameliorates cardiac hypertrophy via activation of eNOS-Nrf2-Tfam pathway in rats

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